Hydrochlorothiazide
- Product NDC
- 50436-3919
- 11-digit product format
- 504363919
- Labeler code
- 50436
- Product ID
- 50436-3919_2ac42df2-d4f7-4a88-a0b1-a2e3ff1f428c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrochlorothiazide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA040807
- Marketing category
- ANDA
- Marketing start
- 2010-08-20
- Marketing end
- 0000-00-00
- Substance
- HYDROCHLOROTHIAZIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record